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首页> 外文期刊>Amino Acids >Using the same organocatalyst for asymmetric synthesis of both enantiomers of glutamic acid-derived Ni(II) complexes via 1,4-additions of achiral glycine and dehydroalanine Schiff base Ni(II) complexes
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Using the same organocatalyst for asymmetric synthesis of both enantiomers of glutamic acid-derived Ni(II) complexes via 1,4-additions of achiral glycine and dehydroalanine Schiff base Ni(II) complexes

机译:使用相同的有机催化剂通过非手性甘氨酸和脱氢丙氨酸席夫碱镍(II)配合物的1,4-加成反应不对称合成谷氨酸衍生的镍(II)配合物的两种对映体

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摘要

(S)- and (R)-BIMBOL were efficient PT catalysts of asymmetric Michael addition of prochiral Ni–PBP–Gly (1) to acrylic esters and malonic esters to Ni–PBP–Δ-Ala (2) correspondingly. The salient feature of the catalysis is opposite configurations of Glu prepared via the two paths with BIMBOL of the same configuration and a perspective novel catalytic procedure for the synthesis of Gla derivatives.
机译:(S)-和(R)-BIMBOL是前手性Ni-PBP-Gly(1)与丙烯酸酯和丙二酸酯向Ni-PBP-Δ-Ala(2)相应地不对称Michael加成的高效PT催化剂。催化的显着特征是通过两条路径用相同构型的BIMBOL制备的Glu的构型相反,并且是合成Gla衍生物的新颖的催化方法。

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